{
    "disease_id": "DOID:206", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:206", 
            "name": "Osteochondromatosis syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:206", 
            "name": "hereditary multiple exostoses 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:206", 
            "name": "hereditary multiple exostoses 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:206", 
            "name": "hereditary multiple exostoses 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:206", 
            "name": "Multiple exostosis syndromes"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:206", 
            "name": "Multiple congenital exostosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:206", 
            "name": "multiple ostechondromas"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007585", 
            "description": "Any exostoses, multiple in which the cause of the disease is a mutation in the EXT1 gene.", 
            "resource": "MONDO", 
            "id": "MONDO:0007585", 
            "name": "exostoses, multiple, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007585", 
            "name": "diaphyseal Aclasis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007585", 
            "name": "exostoses, multiple caused by mutation in EXT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007585", 
            "name": "EXT1 exostoses, multiple"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007585", 
            "name": "multiple osteochondromas"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007585", 
            "name": "EXT"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007585", 
            "name": "osteochondromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007585", 
            "name": "multiple cartilaginous exostoses"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007585", 
            "name": "exostoses, multiple, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007586", 
            "description": "This gene is involved in the heparin/heparin sulfate biosynthesis, cell organization/biogenesis and development of the cytoskeleton in chondrocytes.", 
            "resource": "MONDO", 
            "id": "MONDO:0007586", 
            "name": "exostoses, multiple, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007586", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007586", 
            "name": "exostoses, multiple caused by mutation in EXT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007586", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007586", 
            "name": "EXT2 Gene"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007586", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007586", 
            "name": "exostoses (Multiple) 2 Gene"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007586", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007586", 
            "name": "exostoses, multiple, type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007586", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007586", 
            "name": "EXT2 exostoses, multiple"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007586", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007586", 
            "name": "Ext2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010846", 
            "name": "EXT3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010846", 
            "name": "exostoses, multiple, type III; EXT3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010846", 
            "name": "exostoses, multiple, type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010846", 
            "name": "EXT3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010846", 
            "name": "exostoses, multiple, type 3"
        }, 
        {
            "url": "https://www.omim.org/entry/133700", 
            "description": "Hereditary multiple exostoses 1", 
            "resource": "MIM", 
            "id": "MIM:133700", 
            "name": "Hereditary multiple exostoses 1"
        }, 
        {
            "url": "https://www.omim.org/entry/133701", 
            "description": "Hereditary multiple exostoses 2", 
            "resource": "MIM", 
            "id": "MIM:133701", 
            "name": "Hereditary multiple exostoses 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:206", 
        "description": "An exostosis that has_material_basis_in a mutation on the genes EXT1, EXT2 and EXT3 which results in multiple bony spurs throughout a child's growth.", 
        "resource": "Disease Ontology", 
        "id": "DOID:206", 
        "name": "hereditary multiple exostoses"
    }
}